A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5707953



Internal ID9446199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43072638..43073372hg38UCSC Ensembl
chr1:43538309..43539043hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38735
hg19735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664272
Supporting Variants
SamplesNA18861
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5707953
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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